52764-11-1

Usage

Uses

Used in Pesticide Production:
2,6-dichloropyridin-3-ol is used as an intermediate in the synthesis of various pesticides. Its role in the production process is crucial, as it contributes to the development of effective and efficient pest control solutions.
Used in Chemical Synthesis:
2,6-dichloropyridin-3-ol is used as a building block in the synthesis of other chemical products. Its versatility as a compound allows it to be incorporated into a wide range of applications, making it a valuable component in the chemical industry.
Used in Environmental Applications:
Although 2,6-dichloropyridin-3-ol is not typically found in the environment, its properties and characteristics make it a potential candidate for use in environmental remediation or other ecological applications. Its solubility in water could potentially be utilized in processes that require the interaction with water-based systems.

InChI:InChI=1/C5H3Cl2NO/c6-4-2-1-3(9)5(7)8-4/h1-2,9H

Upstream product

• 2402-78-0 2,6-dichloropyridine 
• 6636-78-8 2-chloro-3-hydroxypyridine 
• 148493-34-9 (2,6-dichloropyridin-3-yl)boronic acid 

Downstream Products

• 1427032-96-9 5-(12-cyano-6H-pyrido[2',3':5,6][1,3]oxazino[3,4-a]indol-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide 
• 1427034-65-8 5-(12-bromo-6H-pyrido[2',3':5,6][1,3]oxazino[3,4-a]indol-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide 
• 1427032-94-7 5-(12-fluoro-6H-pyrido[2',3':5,6][1,3]oxazino[3,4-a]indol-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide 
• 1427032-91-4 5-(12-chloro-6H-pyrido[2',3':5,6][1,3]oxazino[3,4-a]indol-2-yl)-2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide 
• 1418153-04-4 2,6-dichloro-3-ethoxypyridine 
• 1214379-42-6 2,6-dichloro-4-(difluoromethoxy)pyridine 
• 1214349-42-4 2,6-dichloro-3-(difluoromethoxy)pyridine 
• 1214340-74-5 2,6-dichloro-3-methoxypyridine 
• 1426960-32-8 2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(6H-pyrido[2',3':5,6][1,3]oxazino[3,4-a]indol-2-yl)benzofuran-3-carboxamide 

Relevant academic research and scientific papers

TETRACYCLIC HETEROCYCLE COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

TETRACYCLIC HETEROCYCLE COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

TETRACYCLIC HETEROCYCLE COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

Efficient synthesis of halohydroxypyridines by hydroxydeboronation

This paper describes a general method for the synthesis of halohydroxypyridines from novel halopyridinylboronic acids and esters recently described by some of us. Halopyridinylboronic acids and esters have been efficiently hydroxydeboronated under mild conditions by employing hydrogen peroxide or meta-chloroperbenzoic acid. These hydroxylations take place regioselectively without other oxidation (N-oxide formation).

Certain esters of 2-[(2,6-dichloro-3-pyridyl)oxy]propionic acid, compositions containing same and their herbicidal properties

This invention relates to 3-pyridinol compounds corresponding to formula I STR1 wherein A is halogen, alkyl or cyano B is halogen Q is an aliphatic bridge that can also be unsaturated, branched or substituted R is hydrogen, an aliphatic, cycloaliphatic, aromatic or heterocyclic radical, a metal ion or a quaternary ammonium group, Z is oxygen or sulfur, processes for producing them, their use for regulating plant growth, and to compositions containing these compounds.

3-Pyridyl-oxy-alkanecarboxylic acid amides

The present invention relates to 3-pyridyl-oxy-alkancarboxylic acid amides of formula STR1 wherein A and B are individually hydrogen, halogen, alkyl, cyano, nitro or amino, C is hydrogen, halogen or nitro n is 1 or 2 Q is an aliphatic bridge, that can also be branched, unsaturated or substituted, R1 and R2 independently are hydrogen, alkyl, alkoxy, alkenyl, alkynyl, phenyl or benzyl, R1 and R2 together with the nitrogen atom to which they are bound are a 5 to 6 membered heterocycle. The invention also relates to processes for the production of these amides, to their use as regulators of plant growth and as antidotes for herbicides, as well as to compositions containing these amides as active substance.